• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

伴 CNS 累及的 MYD88 突变阳性惰性 B 细胞淋巴瘤:Bing-Neel 综合征的模拟者。

MYD88 mutation-positive indolent B-cell lymphoma with CNS involvement: Bing-Neel syndrome mimickers.

机构信息

Division of Hematology, Ichinomiya Municipal Hospital, Ichinomiya, Japan.

Department of Hematology, Ichinomiya Nishi Hospital, Ichinomiya, Japan.

出版信息

J Clin Exp Hematop. 2024 Sep 28;64(3):252-260. doi: 10.3960/jslrt.24033. Epub 2024 Aug 30.

DOI:10.3960/jslrt.24033
PMID:39218689
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11528247/
Abstract

MYD88 p.L265P mutation occurs in over 90% of Waldenström's macroglobulinemia (WM), which is characterized by lymphoplasmacytic lymphoma (LPL) with monoclonal IgM. WM requires careful diagnosis due to overlapping features with other B-cell malignancies. Bing-Neel syndrome (BNS), a rare complication of WM, involves central nervous system (CNS) invasion. This report describes two cases of morphologically low-grade B-cell lymphoma in the bone marrow accompanied by the presence of a large B-cell lymphoma in the brain and a common MYD88 p.L265P mutation, which were eventually established as BNS mimickers. Although the two components in these cases showed the same identical light-chain restriction, different immunoglobulin heavy-chain rearrangement peaks indicated distinct lymphoma stem cells for CNS and bone marrow lesions. These clinical cases emphasize the challenges in diagnosing BNS. Based on the findings, biopsy is recommended for accurate identification of the clonal relationship and MYD88 mutation status.

摘要

MYD88 p.L265P 突变发生在超过 90%的华氏巨球蛋白血症(WM)中,其特征为单克隆 IgM 的淋巴浆细胞淋巴瘤(LPL)。WM 需要仔细诊断,因为其与其他 B 细胞恶性肿瘤有重叠特征。Bing-Neel 综合征(BNS)是 WM 的一种罕见并发症,涉及中枢神经系统(CNS)侵犯。本报告描述了两例骨髓中形态学低度恶性 B 细胞淋巴瘤伴有脑内大 B 细胞淋巴瘤和常见的 MYD88 p.L265P 突变,最终被确定为 BNS 模拟物。尽管这两个病例的两个成分表现出相同的轻链限制,但不同的免疫球蛋白重链重排峰表明 CNS 和骨髓病变的淋巴瘤干细胞不同。这些临床病例强调了诊断 BNS 的挑战。基于这些发现,建议进行活检以准确识别克隆关系和 MYD88 突变状态。

相似文献

1
MYD88 mutation-positive indolent B-cell lymphoma with CNS involvement: Bing-Neel syndrome mimickers.伴 CNS 累及的 MYD88 突变阳性惰性 B 细胞淋巴瘤:Bing-Neel 综合征的模拟者。
J Clin Exp Hematop. 2024 Sep 28;64(3):252-260. doi: 10.3960/jslrt.24033. Epub 2024 Aug 30.
2
MYD88 L265P somatic mutation in Waldenström's macroglobulinemia.瓦尔登斯特伦巨球蛋白血症中的 MYD88 L265P 体细胞突变。
N Engl J Med. 2012 Aug 30;367(9):826-33. doi: 10.1056/NEJMoa1200710.
3
MYD88 L265P mutation contributes to the diagnosis of Bing Neel syndrome.MYD88 L265P 突变有助于宾-尼尔综合征的诊断。
Br J Haematol. 2014 Nov;167(4):506-13. doi: 10.1111/bjh.13078. Epub 2014 Aug 27.
4
[Lymphoplasmacytic lymphoma accompanied by transformed diffuse large B-cell lymphoma with the MYD88 mutation].伴有转化型弥漫性大B细胞淋巴瘤及MYD88突变的淋巴浆细胞淋巴瘤
Rinsho Ketsueki. 2017;58(2):155-160. doi: 10.11406/rinketsu.58.155.
5
MYD88 L265P somatic mutation: its usefulness in the differential diagnosis of bone marrow involvement by B-cell lymphoproliferative disorders.MYD88 L265P 体细胞突变:在 B 细胞淋巴增殖性疾病骨髓累及的鉴别诊断中的作用。
Am J Clin Pathol. 2013 Sep;140(3):387-94. doi: 10.1309/AJCP10ZCLFZGYZIP.
6
Clone-specific MYD88 L265P and CXCR4 mutation status can provide clinical utility in suspected Waldenström macroglobulinemia/lymphoplasmacytic lymphoma.克隆特异性的MYD88 L265P和CXCR4突变状态可为疑似华氏巨球蛋白血症/淋巴浆细胞淋巴瘤提供临床应用价值。
Leuk Res. 2016 Dec;51:41-48. doi: 10.1016/j.leukres.2016.10.008. Epub 2016 Oct 18.
7
[IgG-variant Bing-Neel syndrome diagnosed by detecting MYD88 L265P mutation in the cerebrospinal fluid cells].通过检测脑脊液细胞中的MYD88 L265P突变诊断IgG变异型宾-尼尔综合征
Rinsho Ketsueki. 2021;62(10):1493-1498. doi: 10.11406/rinketsu.62.1493.
8
L265P mutation of the MYD88 gene is frequent in Waldenström's macroglobulinemia and its absence in myeloma.MYD88 基因的 L265P 突变在华氏巨球蛋白血症中很常见,而在骨髓瘤中则不存在。
PLoS One. 2013 Nov 5;8(11):e80088. doi: 10.1371/journal.pone.0080088. eCollection 2013.
9
MYD88 L265P mutation analysis is a useful diagnostic adjunct for lymphoplasmacytic lymphoma with pleural effusion.对伴有胸腔积液的淋巴浆细胞淋巴瘤进行 MYD88 L265P 突变分析有助于明确诊断。
Pathol Int. 2019 Oct;69(10):601-607. doi: 10.1111/pin.12854. Epub 2019 Sep 25.
10
Pleural fluid MYD88 L265P mutation supporting diagnosis and decision to treat extramedullary Waldenstrom's macroglobulinemia: a case report.支持诊断和决定治疗骨髓外华氏巨球蛋白血症的胸腔液 MYD88 L265P 突变:一例报告。
J Med Case Rep. 2020 Jul 13;14(1):98. doi: 10.1186/s13256-020-02404-x.

引用本文的文献

1
Background and Clinical Features of a Unique and Mysterious Autoinflammatory Disease, Schnitzler Syndrome.一种独特且神秘的自身炎症性疾病——施尼茨勒综合征的背景与临床特征
Int J Mol Sci. 2025 Jan 12;26(2):598. doi: 10.3390/ijms26020598.

本文引用的文献

1
Lymphoplasmacytic lymphoma and marginal zone lymphoma involving bone marrow: A diagnostic dilemma. Useful clinicopathological features to accurate the diagnosis.累及骨髓的淋巴浆细胞性淋巴瘤和边缘区淋巴瘤:诊断难题。有助于准确诊断的临床病理特征。
EJHaem. 2022 Oct 5;3(4):1181-1187. doi: 10.1002/jha2.573. eCollection 2022 Nov.
2
Diagnostics in Waldenström's macroglobulinemia: a consensus statement of the European Consortium for Waldenström's Macroglobulinemia.华氏巨球蛋白血症的诊断:欧洲华氏巨球蛋白血症联盟共识声明。
Leukemia. 2023 Feb;37(2):388-395. doi: 10.1038/s41375-022-01762-3. Epub 2022 Nov 26.
3
The Impact of Tirabrutinib Monotherapy for Bing-Neel Syndrome in Waldenström's Macroglobulinemia.
替雷利珠单抗单药治疗华氏巨球蛋白血症中宾-尼尔综合征的疗效
Intern Med. 2022 Dec 1;61(23):3473-3474. doi: 10.2169/internalmedicine.0041-22. Epub 2022 May 14.
4
Bing-Neel Syndrome: An Initial Manifestation of Waldenstrom Macroglobulinemia.宾-尼尔综合征:华氏巨球蛋白血症的首发表现
Cureus. 2021 Nov 9;13(11):e19402. doi: 10.7759/cureus.19402. eCollection 2021 Nov.
5
Lymphoplasmacytic lymphoma associated with diffuse large B-cell lymphoma: Progression or divergent evolution?淋巴浆细胞淋巴瘤伴弥漫大 B 细胞淋巴瘤:进展还是不同的演化?
PLoS One. 2020 Nov 12;15(11):e0241634. doi: 10.1371/journal.pone.0241634. eCollection 2020.
6
Phase I/II study of tirabrutinib, a second-generation Bruton's tyrosine kinase inhibitor, in relapsed/refractory primary central nervous system lymphoma.替拉鲁替尼(第二代布鲁顿酪氨酸激酶抑制剂)治疗复发/难治性原发性中枢神经系统淋巴瘤的 I/II 期研究。
Neuro Oncol. 2021 Jan 30;23(1):122-133. doi: 10.1093/neuonc/noaa145.
7
Clinical significance of disease-specific MYD88 mutations in circulating DNA in primary central nervous system lymphoma.原发性中枢神经系统淋巴瘤循环DNA中疾病特异性MYD88突变的临床意义
Cancer Sci. 2018 Jan;109(1):225-230. doi: 10.1111/cas.13450. Epub 2017 Dec 23.
8
Guideline for the diagnosis, treatment and response criteria for Bing-Neel syndrome.宾-尼尔综合征的诊断、治疗及反应标准指南。
Haematologica. 2017 Jan;102(1):43-51. doi: 10.3324/haematol.2016.147728. Epub 2016 Oct 6.
9
Successful Treatment of Bing-Neel Syndrome Accompanying Waldenström's Macroglobulinemia with R-MPV: A Case Report.R-MPV成功治疗伴发华氏巨球蛋白血症的宾-尼尔综合征:一例报告
J Clin Exp Hematop. 2015;55(2):113-9. doi: 10.3960/jslrt.55.113.
10
Bing-Neel syndrome, a rare complication of Waldenström macroglobulinemia: analysis of 44 cases and review of the literature. A study on behalf of the French Innovative Leukemia Organization (FILO).宾-尼尔综合征,一种华氏巨球蛋白血症的罕见并发症:44例病例分析及文献综述。一项代表法国创新白血病组织(FILO)开展的研究。
Haematologica. 2015 Dec;100(12):1587-94. doi: 10.3324/haematol.2015.133744. Epub 2015 Sep 18.